Diamedix Immunosimplicity Ana (Is-Ana) Screen Test System
FDA 510(k) K980337 · Helix Diagnostics, Inc.
510(k) numberK980337
Submission
- Device name
- Diamedix Immunosimplicity Ana (Is-Ana) Screen Test System
- Applicant
- Helix Diagnostics, Inc.
West Sacramento, CA, US - Received
- January 28, 1998
- Decision date
- May 12, 1998
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- LJM – Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.5100
- Specialty
- Immunology
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|---|---|---|---|
| K182353 | EliA CENP Immunoassay, EliA U1RNP Immunoassay, EliA RNP70 ImmunoassayLJM · Traditional | Phadia AB | 11/27/2018SE |
| K151559 | ImmuLisa Enhanced Centromere Antibody ELISALJM · Traditional | Immco Diagnostics, Inc. | 03/11/2016SE |
| K140493 | Elia SCL-70S ImmunoassayLJM · Traditional | Phadia GmbH | 10/30/2014SE |
| K123880 | Quanta Flash CentromereLJM · Traditional | Inova Diagnostics, Inc. | 02/07/2014SE |
| K131330 | Gold Standard Diagnostics Anti-Nuclear Antibody (Ana) Screen Elisa Test KitLJM · Traditional | Gold Standard Diagnostics | 01/28/2014SE |
| K131185 | Ana Screen Elisa (Igg)LJM · Traditional | Euroimmun US | 07/15/2013SE |
| K083188 | Varelisa Recombi Ana Screen, Model 12 596LJM · Traditional | Phadia US, Inc. | 03/13/2009SE |
| K050967 | Varelisa Recombi CTD Screen, Model 13096LJM · Traditional | Sweden Diagnostics (Germany) GmbH | 06/28/2005SE |
| K050625 | Varelisa Recombi Ana Profile, Model 18496LJM · Traditional | Sweden Diagnostics (Germany) GmbH | 04/26/2005SE |
| K041102 | Immulisa Antinuclear Antibody Screen ElisaLJM · Traditional | Immco Diagnostics, Inc. | 10/26/2004SE |
More from Immco Diagnostics, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K001900 | Enzyme Immunoassay Anti-Ssdna Antibody TestLRM · Traditional | 09/11/2000SE |
| K000489 | Enzyme Immunoassay Anti-Centromere Antibody TestLLL · Traditional | 04/05/2000SE |
| K960091 | Enzyme Immunoassay Anti-Double Stranded DNA (Dsdna) Test KitLRM · Traditional | 03/20/1996SE |
| K954723 | Enzyme Immunoassay Ana Screening Test KitLKJ · Traditional | 12/15/1995SE |
| K954700 | Enzyme Immunoassay Lupus Screen Test KitLKJ · Traditional | 12/15/1995SE |
| K952253 | Enzyme Immunoassay Ena Plus Screening Test KitLLL · Traditional | 08/24/1995SE |
| K951850 | Enzyme Immunoassay ANTI-JO-1 Antibody Test KitLJM · Traditional | 07/18/1995SE |
| K951798 | Enzyme Immunoassay ANTI-SCI-70 Antibody Test KitLJM · Traditional | 07/17/1995SE |
| K940588 | Enzyme Immunoassay Anti-Sm/Rnp Antibody Test KitLKO · Traditional | 04/20/1994SE |
| K940510 | Enzyme Immunoassay Anti-Sm Antibody Test KitLKP · Traditional | 04/20/1994SE |
Questions and answers
When was Diamedix Immunosimplicity Ana (Is-Ana) Screen Test System cleared by the FDA?
Diamedix Immunosimplicity Ana (Is-Ana) Screen Test System (K980337) received a 510(k) decision of Substantially Equivalent on May 12, 1998, 104 days after the submission was received.
What is the product code of K980337?
The FDA product code is LJM – Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls, a Class II (moderate risk) device regulated under 21 CFR 866.5100.